Results 91 to 100 of about 2,479 (192)

The العلاقة بين التعدد الشكلي لجينة NUDT15 ذات الرقم ( rs116855232 ) والسمية النقوية المحرضة بمركبات البورين Mercaptopurine عند المرضى السوريين المشخص لديهم ابيضاض لمفاوي حاد

open access: yesمجلة جامعة دمشق للعلوم الطبية, 2021
Background and Aims: NUDT15 genetic polymorphism is known to be associated with frequent hematopoietic toxicities during acute lymphoblastic leukemia (ALL) mercaptopurine therapy.
محمد ماجد محمد
doaj  

ال طفرة جينة NUDT15 R139C تزيد من خطورة تطور سمية محرضة بمركبات mercaptopurine عند مريضة سورية: تقرير حالة

open access: yesمجلة جامعة دمشق للعلوم الطبية, 2022
خلفية البحث وهدفه: يعد دواء المركابتوبورين mercaptopurine (6MP) حجر الأساس في علاج مرضى الابيضاض اللمفاوي الحاد ولاسيما في مرحلة الصيانة. إن الهدف من عرض هذه الحالة هو إيضاح أسباب تطور تثبيط نقوي شديد عند مريضة مشخص لها ابيضاض لمفاوي حاد ولاسيما ...
محمد محمد, ماهر سيفو
doaj  

The Nudix Hydrolase 15 (NUDT15) Gene Variants among Jordanian Arab Population [PDF]

open access: yesAsian Pacific Journal of Cancer Prevention, 2019
Background: Nudix Hydrolase 15 gene (NUDT15) encodes nucleotide triphosphate diphosphatase which metabolizes the purine analog drugs, such as anticancer thiopurine and anti-gout allopurinol. Genetic variants on Nudix Hydrolase 15 gene (NUDT15) gene effects the drug’s hydrolyses and hence increases the susceptibility to drug-induced toxicity. The NUDT15
Jarrar, Yazun Bashir, Ghishan, Maria
openaire   +2 more sources

Alopecia as an Early Clinical Marker for Azathioprine Induced Myelosuppression: A Case Report [PDF]

open access: yes
Azathioprine is a pro-drug and is metabolized by the TPMT enzyme in the body. In South Asians, Azathioprine is known to cause alopecia and bone marrow suppression in patients with TPMT enzyme deficiency.
Babu, Dr. M Suresh, , Professor   +3 more
core   +2 more sources

Ten years of Genome Medicine. [PDF]

open access: yes, 2019
This year marks the 10th anniversary of Genome Medicine. The journal was launched to meet the need in the community for a platform to publish impactful and open science that advances basic and clinical research—using genetic, genomic, omic, and systems ...
Auffray, C   +4 more
core   +1 more source

Predictive Value of NUDT15 Variants on Neutropenia Among Han Chinese Patients with Dermatologic Diseases: A Single-Center Observational Study

open access: yesDermatology and Therapy, 2020
Introduction Azathioprine is a synthetic purine analogue derived from 6-mercaptopurine which acts by disrupting nucleic acid synthesis and interfering with T cell activation. It is effective in dermatology diseases related to the immune system.
Po-Wei Huang   +2 more
doaj   +1 more source

Insights Into Patient‐Level Exposure to Actionable Pharmacogenomic Medications in Australia Using a New National Pharmacogenomic Guideline

open access: yesClinical Pharmacology &Therapeutics, Volume 119, Issue 1, Page 89-100, January 2026.
This study assessed the use of 35 pharmacogenomic (PGx) medications listed in the Royal College of Pathologists of Australasia (RCPA) guideline, estimated the potential costs of subsidizing PGx testing in Australia, and predicted related prescribing changes.
Bella D. Ianni   +3 more
wiley   +1 more source

Identification and expression analysis of peroxisome-targeted defence proteins mediating innate immunity in the model plant Arabidopsis thaliana [PDF]

open access: yes, 2011
Master's thesis in Biological ChemistryPeroxisomes are single-membrane organelles that have oxidative metabolic functions. Peroxisomes carry out major functions such as lipid degradation, photorespiration and glyoxylate cycle. However, new functions have
Mwaanga, Chimuka
core  

Star Allele-Based Haplotyping versus Gene-Wise Variant Burden Scoring for Predicting 6-Mercaptopurine Intolerance in Pediatric Acute Lymphoblastic Leukemia Patients

open access: yesFrontiers in Pharmacology, 2019
Nudix Hydrolase 15 (NUDT15) and Thiopurine S-Methyltransferase (TPMT) are strong genetic determinants of thiopurine toxicity in pediatric acute lymphoblastic leukemia (ALL) patients.
Yoomi Park   +11 more
doaj   +1 more source

Homozygote CRIM1 variant is associated with thiopurine-induced neutropenia in leukemic patients with both wildtype NUDT15 and TPMT

open access: yesJournal of Translational Medicine, 2020
Background NUDT15 and TPMT variants are strong genetic determinants of thiopurine-induced hematological toxicity that results in therapeutic failure in pediatric acute lymphoblastic leukemia (ALL).
Yoomi Park   +11 more
doaj   +1 more source

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